3,6-dichloropyridazine

Clc1cc(C2CCC2)c(Cl)nn1
Reaction #11321
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NNc1ccc(Cl)nn1
Reaction #40721
1-(6-chloropyridazin-3-yl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1C[C@H]2CCN(c3ccc(N4CCN(c5ccc(Cl)nn5)CC4)cc3)[C@H]2C1
Reaction #41242
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc(OCc2ccccc2)nn1
Reaction #51038
3-benzyloxy-6-chloro-pyridazine
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(N)c1ccc(Cl)nn1
Reaction #67582
N-(6-Chloro-pyridazin-3-yl)-N-methyl-hydrazine
収率 53.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
FC(F)(c1ccc2ncccc2c1)c1nnc2ccc(Cl)nn12
Reaction #68661
6-((6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)difluoromethyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(-c2ccc(Cl)nn2)sn1
Reaction #68663
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=CC1=CC=C(Cl)NN1c1cc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl
Reaction #74483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC[CH2][SnH]([CH2]CCC)[CH2]CCC.Clc1ccc(Cl)nn1
Reaction #82703
3,6-dichloropyridazine tributylstannane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1ccc(Oc2ccc(Cl)nn2)cc1
Reaction #95436
4-(6-chloro-3-pyridazinyloxy)benzeneamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cc1cc(Oc2ccc(Cl)nn2)c(C)cc1N
Reaction #95437
4-(6-chloro-3-pyridazinyloxy)-2,5-dimethylbenzeneamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Nc1cccc(Oc2ccc(Cl)nn2)c1
Reaction #95438
3-(6-chloro-3-pyridazinyloxy)benzeneamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C[C@@H]1CN(c2ccc(Cl)nn2)CCN1C(=O)OC(C)(C)C
Reaction #166290
compound 11
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ccc(Nc2ncc3c4ccncc4n(C4CCCC4)c3n2)nn1
Reaction #166307
compound 140
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ncc(-c2cc(Cl)nnc2Cl)c(NC2CCCC2)n1
Reaction #166378
Compound 323
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1CCOC2(CCN(c3ccc(Cl)nn3)CC2)C1
Reaction #166417
compound 406
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ccc(N2CC3CC4CC2CN(C4)C3)nn1
Reaction #167601
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCCCN1CCN(c2ccc(Cl)nn2)CC1
Reaction #167921
3-[4-(6-chloropyridazin-3-yl)piperazin-1-yl]propan-1-ol
収率 50.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2ccc(Cl)nn2)cc1
Reaction #181059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CC2CCN(c3ccc(N4CCN(c5ccc(Cl)nn5)CC4)cc3)C2C1
Reaction #181720
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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